22 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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FORTIFY ASSURA DR ICD, US
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·June 13, 2016
FORTIFY ASSURA VR ICD_IDE_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017
ELLIPSE VR ICD
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017
CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017
SMALL PERIPHERAL CUTTING BALLOON
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code NWX·August 19, 2019
FORTIFY ASSURA VR ICD_IDE_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017
UNIFY ASSURA CRT-D RF HV
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·March 29, 2019
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 11, 2013
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·November 10, 2010
PINN CAN BONE SCREW 6.5MMX25MM
FDA Adverse Event
Injury
·JOHNSON & JOHNSON MEDICAL(SUZHOU)LTD.3006356043·Product code NDJ·July 2, 2014
FORTIFY ST DR, U1.6 SJ4 ID
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017
FORTIFYASSURA DR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017
FORTIFY ASSURA VR ICD_O_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 27, 2016
SMALL PERIPHERAL CUTTING BALLOON
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code LOX·May 5, 2011
COMPREHENSIVE REVERSE SHOULDER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·December 30, 2016
COMPREHENSIVE REVERSE SHOULDER-MINI BASEPLATE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·December 30, 2016
COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW 3.5MM HEX 4.75 X1 5MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·September 21, 2016
COMPREHENSIVE REVERE SHOULDER FIXED LOCKING SCREW 3.5MM HEX 4.75 X 20MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·September 21, 2016
COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW 6.5MM X 35MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·September 21, 2016
COMP LK SCR 3.5HEX 4.75X15 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·June 1, 2018